Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46323837-46324202 | Common:2; Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
chr21:46635472-46635726 | Common:5; Rare:84 | ||||
chr22:17159197-17159385 | Common:4; Rare:91 | ||||
chr22:17628694-17628860 | Common:1; Rare:55 | ||||
chr22:17638684-17638817 | Rare:46 | ||||
chr22:18077802-18078007 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
chr22:19122392-19122678 | Common:3; Rare:65 | ||||
chr22:19432380-19432599 | Common:2; Rare:91 | ||||
chr22:19447667-19447914 | Common:2; Rare:103 | ||||
chr22:19854795-19854972 | Rare:61 | ||||
chr22:19941722-19941877 | Rare:66; Clinvar:5; Clinvar (benign):4 | ||||
chr22:20020873-20021125 | Common:1; Rare:82 | ||||
chr22:20319998-20320158 | Common:1; Rare:53 | ||||
chr22:20495781-20495905 | Common:1; Rare:48 | ||||
chr22:20917228-20917423 | Rare:68 |